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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137157inversion1nstd234human GRCh37 chrX: 31,626,542-82,320,140 , GRCh38.p12 chrX: 31,608,425-83,065,132 ABCB7, ACTG1P10, 775 more genes
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098786copy number variation1nstd102humanPathogenic GRCh37 chrX: 46,466,387-51,241,672 , GRCh38.p12 chrX: 46,606,952-51,498,820 LOC100419232, LOC791091, 172 more genes
    nsv7098319copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chrX: 48,368,209-51,241,672 , GRCh38.p12 chrX: 48,509,821-51,498,820 GRIPAP1, ASMER2, 92 more genes
    nsv7098318copy number variation3nstd102humanUncertain significance GRCh37 chrX: 47,001,716-50,659,607 , GRCh38.p12 chrX: 47,142,317-50,916,607 PYY3, CCDC120, 148 more genes
    nsv7098317copy number variation1nstd102humanPathogenic GRCh37 chrX: 46,466,387-50,659,607 , GRCh38.p12 chrX: 46,606,952-50,916,607 PLP2, RN7SL262P, 160 more genes
    nsv7088019copy number variation1nstd229human GRCh38 chrX: 48,984,801-49,307,700 , GRCh37.p13 chrX: 48,841,214-49,164,179 , GRCh37.p13 chrX|NW_004070880.2: 1,224,230-1,547,129 CCDC120, GRIPAP1, 19 more genes
    nsv7088018copy number variation1nstd229human GRCh38 chrX: 48,971,001-49,001,500 , GRCh37.p13 chrX|NW_004070880.2: 1,210,430-1,240,929 , GRCh37.p13 chrX: 48,827,408-48,857,911 GRIPAP1, KCND1
    nsv7088012copy number variation1nstd229human GRCh38 chrX: 48,891,201-49,305,700 , GRCh37.p13 chrX|NW_004070880.2: 1,130,630-1,545,129 , GRCh37.p13 chrX: 48,748,484-49,162,179 GPKOW, GRIPAP1, 26 more genes
    nsv7088011copy number variation1nstd229human GRCh38 chrX: 48,891,201-49,249,700 , GRCh37.p13 chrX|NW_004070880.2: 1,130,630-1,489,129 , GRCh37.p13 chrX: 48,748,484-49,106,161 HSPB1P2, PRAF2, 23 more genes
    nsv7088003copy number variation1nstd229human GRCh38 chrX: 48,826,501-49,260,900 , GRCh37.p13 chrX|NW_004070880.2: 1,065,930-1,500,329 , GRCh37.p13 chrX: 48,684,911-49,117,357 RN7SL262P, PIM2, 25 more genes
    nsv7088001copy number variation1nstd229human GRCh38 chrX: 48,785,001-49,009,000 , GRCh37.p13 chrX: 48,643,409-48,865,410 , GRCh37.p13 chrX|NW_004070880.2: 1,024,430-1,248,429 RNU6-722P, ERAS, 10 more genes
    nsv7088000copy number variation1nstd229human GRCh38 chrX: 48,784,801-49,271,500 , GRCh37.p13 chrX: 48,643,209-49,127,962 , GRCh37.p13 chrX|NW_004070880.2: 1,024,230-1,510,929 GPKOW, CCDC120, 29 more genes
    nsv7030254inversion1nstd229human GRCh38 chrX: 48,980,431-48,980,533 , GRCh37.p13 chrX|NW_004070880.2: 1,219,860-1,219,962 , GRCh37.p13 chrX: 48,836,844-48,836,946 GRIPAP1
    nsv7028188inversion1nstd229human GRCh38 chrX: 48,271,055-52,545,048 , GRCh37.p13 chrX|NW_004070877.1: 1-2,258,163 SSXP8, CACNA1F, 141 more genes
    nsv6637069copy number variation1nstd102humanPathogenic GRCh37 chrX: 39,525,562-52,832,596 , GRCh38.p12 chrX: 39,666,308-52,803,572 LOC100419238, NDP, 312 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6315577complex substitution1nstd102humanPathogenic GRCh37 chrX: 590,376-56,315,041 , GRCh38.p12 chrX: 629,641-56,288,608 ACTG1P10, NR0B1, 778 more genes
    nsv6315393copy number variation1nstd102humanPathogenic GRCh37 chrX: 61,545-155,226,048 , GRCh38.p12 chrX: 11,545-155,996,383 H2BP8, LOC101060199, 2151 more genes
    nsv6315389copy number variation1nstd102humanPathogenic GRCh37 chrX: 11,522,765-155,233,731 , GRCh38.p12 chrX: 11,504,645-156,004,066 RBMX, LOC100129144, 2042 more genes
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